rs727505159

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs727505159(C;T)

Make rs727505159(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

74114804

Gene

VCL

is a	snp
is	mentioned by
dbSNP	rs727505159
dbSNP (classic)	rs727505159
ClinGen	rs727505159
ebi	rs727505159
HLI	rs727505159
Exac	rs727505159
Gnomad	rs727505159
Varsome	rs727505159
LitVar	rs727505159
Map	rs727505159
PheGenI	rs727505159
Biobank	rs727505159
1000 genomes	rs727505159
hgdp	rs727505159
ensembl	rs727505159
geneview	rs727505159
scholar	rs727505159
google	rs727505159
pharmgkb	rs727505159
gwascentral	rs727505159
openSNP	rs727505159
23andMe	rs727505159
SNPshot	rs727505159
SNPdbe	rs727505159
MSV3d	rs727505159
GWAS Ctlg	rs727505159

Max Magnitude

0

ClinVar
Risk	rs727505159(T;T)
Alt	rs727505159(T;T)
Reference	Rs727505159(C;C)
Significance	Probable-Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	VCL
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000010.10:g.75874562C>T
CLNSRC
CLNACC	RCV000156630.1,